Evidence map›Paper›PMID 29632354›Full record

ArticleNature ecology & evolution2018

Multicopy plasmids allow bacteria to escape from fitness trade-offs during evolutionary innovation.

Jeronimo Rodriguez-Beltran, J Carlos R Hernandez-Beltran, Javier DelaFuente, Jose A Escudero, Ayari Fuentes-Hernandez, R Craig MacLean, Rafael Peña-Miller, Alvaro San Millan

Abstract read
In one paragraph

Article in Nature ecology & evolution, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed.

  1. Article
  2. Article
  3. Heterogeneous multicopy of blaNature communications · 2026
    Article
  4. Plasmid mutation rates scale with copy number.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The extended mobility of plasmids.Nucleic acids research · 2025
    Review
  11. Article
  12. Article
  13. The metabolic burden associated with plasmid acquisition: An assessment of the unrecognized benefits to host cells.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jeronimo Rodriguez-BeltranDepartment of Microbiology, Hospital Universitario Ramon y Cajal (IRYCIS), Madrid, Spain. jeronimo.rodriguez.beltran@gmail.com.ORCID http://orcid.org/0000-0003-3014-1229
J Carlos R Hernandez-BeltranCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Morelos, Mexico.
Javier DelaFuenteDepartment of Microbiology, Hospital Universitario Ramon y Cajal (IRYCIS), Madrid, Spain.
Jose A EscuderoDepartamento de Sanidad Animal and VISAVET, Facultad de Veterinaria, Universidad Complutense de Madrid, Madrid, Spain.
Ayari Fuentes-HernandezCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Morelos, Mexico.
R Craig MacLeanDepartment of Zoology, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-7941-813X
Rafael Peña-MillerCentro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Morelos, Mexico.
Alvaro San MillanDepartment of Microbiology, Hospital Universitario Ramon y Cajal (IRYCIS), Madrid, Spain. alvsanmillan@gmail.com.ORCID http://orcid.org/0000-0001-8544-0387

Funding

Wellcome Trust
6 · The paper itself

Abstract

Understanding the mechanisms governing innovation is a central element of evolutionary theory. Novel traits usually arise through mutations in existing genes, but trade-offs between new and ancestral protein functions are pervasive and constrain the evolution of innovation. Classical models posit that evolutionary innovation circumvents the constraints imposed by trade-offs through genetic amplifications, which provide functional redundancy. Bacterial multicopy plasmids provide a paradigmatic example of genetic amplification, yet their role in evolutionary innovation remains largely unexplored. Here, we reconstructed the evolution of a new trait encoded in a multicopy plasmid using TEM-1 β-lactamase as a model system. Through a combination of theory and experimentation, we show that multicopy plasmids promote the coexistence of ancestral and novel traits for dozens of generations, allowing bacteria to escape the evolutionary constraints imposed by trade-offs. Our results suggest that multicopy plasmids are excellent platforms for evolutionary innovation, contributing to explain their extreme abundance in bacteria.

Indexed as

Biological EvolutionGenetic FitnessBacteriabeta-LactamasesEscherichia coliModels, BiologicalPhenotypePlasmidsbeta-Lactamasesbeta-lactamase TEM-1

Identifiers

PMID29632354
PMCPMC6055991

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.